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REVISION OF FEVILLEA (CUCURBITACEAE: ZANONIEAE)
George L. Robinson
Richard P. Wunderlin
USDA APHIS, Plant Protection and Quarantine
Port Everglades
1800 Eller Drive, Suite 414
Fort Lauderdale, Florida 33316, U.S.A.
Department of Biology, SCA 110
University of South Florida
Tampa, Florida 33620-5200, U.S.A.
ABSTRACT
A revision of the neotropical genus Fevillea with keys, descriptions, and distribution is provided.
Two subgenera are recognized: subgenus Fevillea with six species and subgenus Anisosperma with
one species. Fevillea bahiensis G. Robinson & Wunderlin from Brazil is described as new and subgenus Anisosperma (Silva Manso) G. Robinson & Wunderlin is proposed.
RESUMEN
Se aporta una revisión del género neotropical Fevillea con claves, descripciones, y distribución. Se
reconocen dos subgéneros: subgénero Fevillea con seis especies y subgénero Anisosperma con una
especie. Se describe como nueva Fevillea bahiensis G. Robinson & Wunderlin de Brasil y se propone
el subgénero Anisosperma (Silva Manso) G. Robinson & Wunderlin.
Fevillea (Cucurbitaceae: Zanonieae), a neotropical genus of seven species, is
characterized by leaves with glands, calyx with glandular squamellae (except
F. passiflora), petals with a medial adaxial flap-like appendage or ridge, staminate flowers with five bilocular anthers, and a globose, usually indehiscent,
large-seeded fruit.
TAXONOMIC HISTORY
Fevillea was established by Linnaeus (1753) in honor of Louis Éconches Feuillée,
(1660–1732), a French clergyman, explorer, astronomer, and botanist. Linnaeus
recognized two species, F. trilobata and F. cordifolia.
Adanson (1763) published the pre-Linnaean name Nhandiroba, of
Marcgrave (Piso & Marcgrave 1648), but placed Linnaeus’s name Fevillea in
synonymy, thereby making Nhandiroba illegitimate. No species were listed. The
name Nhandiroba remained unused until resurrected by Kuntze (1891–1898).
The first comprehensive treatment of Fevillea since Linnaeus (1753) was
that of Seringe (1828) who recognized four species. In addition to F. cordifolia
and F. trilobata, Seringe recognized F. punctata (L.) Poir. [=Trichosanthes sp.] and
F. javilla Kunth [=F. cordifolia].
Silva Manso (1836) established the monotypic Hypanthera with H. guapeva
[=Fevillea trilobata] and Anisosperma with A. passiflora (Vell.) Silva Manso
[=Fevillea passiflora Vell.]. Both monotypic genera were accepted by most subsequent workers until recently.
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Roemer (1846) recognized Hypanthera and Fevillea. He placed ten species
in Fevillea, incorporating some taxa now placed in Trichosanthes L., Pteropepon
Cogn., and Sicydium Schltdl. Fevillea passiflora was also recognized, but without reference to Silva Manso’s placement of the species in Anisosperma. Roemer
erected two sections: section Fevillea with nine species and section Javilla with
only F. javilla Kunth [=F. cordifolia L.].
Cogniaux (1878) recognized three species of Fevillea for Brazil: F. trilobata,
F. albiflora Cogn., and F. deltoidea Cogn. (the latter now in Pteropepon). In addition, he recognized the monotypic genus Anisosperma and expanded the generic limits of the previously Old World genus Alsomitra (Blume) M. Roem. to
include two new neotropical species: A. brasiliensis [=Siolmatra brasiliensis
(Cogn.) Baill.] and A. pedatifolia [=Fevillea pedatifolia (Cogn.) C. Jeffrey]. In a
more comprehensive treatment, Cogniaux (1881) expanded Fevillea to six species, maintaining Anisosperma and Alsomitra.
The genus Siolmatra, a segregate of Alsomitra created by Baillon (1885) to
acommodate Alsomitra brasiliensis Cogn. [=Siolmatra brasiliensis (Cogn.)
Baill.], was accepted by Cogniaux (1893) who described a second species (S.
paraguayensis). Three additional species were later added by Cogniaux (1916),
one new (S. amazonica) and two transferred from Alsomitra (S. pedatifolia
(Cogn.) Cogn. and S. peruviana (Huber) Cogn.). Harms (1926) added a sixth species (S. pentaphylla), later (Harms 1933) a seventh (S. simplicifolia), and Standley
(1937) an eighth (S. mexiae). Jeffrey (1962b), noting the incongruent mixture of
taxa in Siolmatra, recircumscribed the genus and transferred four species to
Fevillea. In reviewing the New World taxa of the Cucurbitaceae, Jeffrey (1978)
listed nine species in Fevillea, including F. passiflora, considering Anisosperma
congeneric with Fevillea.
FLORAL AND FRUIT MORPHOLOGY
The staminate inflorescence consists of numerous, small, pentamerous flowers that are paniculate in subgenus Fevillea or fasciculate to subumbelliform
in subgenus Anisosperma.
In subgenus Fevillea, the midrib of the adaxial surface of the sepals is fused
with the lower margins of the petals. At or above this point of fusion extends a
small glandular protuberance of uncertain ontogenic origin which is here referred to as a “glandular calycine squamella.” The exudate from the squamellae
is clear and remains visible on most herbarium specimens. Each petal has a
median, adaxial, uncinate appendage or slightly raised glandular midrib which
is adnate with the base of the stamen filament. In subgenus Anisosperma, the
sepals and petals are united at their base and lack squamellae. Instead, the petals have a median, adaxial, glandular ridge.
An articulation occurs between the filiform hypanthium and the pedicel.
The indumentum on the staminate flowers is quite variable in most species and
ROBINSON AND WUNDERLIN, REVISION OF FEVILLEA
1973
is similar (when present) on both the hypanthium and pedicel. However, F.
trilobata has a stipitate-glandular pubescence on the hypanthium above the
articulation in rather sharp contrast to the non-glandular trichomes on the
pedicel below.
The presence of five free, bilocular anthers in Fevillea is unique for the family and is considered plesiomorphic. The general trend within the Cucurbitaceae
is the reduction of stamen number from five to three or to two and the reduction in locule number from two to one.
The pistillate flowers are rarely collected and are thus imperfectly known
or unknown for some species. We have seen them in only four of the seven species. Those of F. pergamentacea and F. passiflora are known to us only through
the literature while those of F. moorei are unknown.
The petals of the pistillate flowers have a slightly raised median appendage extending from the base to the center, reminiscent of those of the staminate
flowers. Two small glands occur at the base of the petal on either side of this
median appendage. A large, subrotund, flattened, glandular protuberance extends from the base of the calyx lobe between each petal. These protuberances
may represent staminodes. Cogniaux (1878, 1881, 1916) reported these structures,
counting 20 small “glands” at the base of the petals. This probably included the
sum total of glands, ridges, and protuberances.
The fruits of subgenus Fevillea are large, subglobose, mottled green or
brown, and gourd-like. The size ranges from 8 to 16 cm in length and from 7 to
13 cm in diameter. An individual plant may produce as many as 50 to 100 fruits
at a time (Gentry & Wettach 1986). The fleshy rind of the fruit is zonate above
the middle with the hypanthium lip scar (ovary partly inferior). The fruits are
typically indehiscent, but reportedly sometimes dehiscent along the hypanthium lip scar in F. pedatifolia (A. Gentry, pers. comm.). In contrast, the fruits
of subgenus Anisosperma are ovoid or oblong, subtrigonous, short-apiculate at
the apex, and not zonate above the middle (ovary fully inferior). The seeds (up
to 15 per fruit) vary from 3 to 6 cm in diameter and weigh 3 to 9 g when dry.
They are among the largest in the Cucurbitaceae and are comparable in size
only to those of the paleotropical genera Telfairia (Cucurbitoideae: Joliffieae)
and Hodgsonia (Cucurbitoideae: Trichosantheae). The seed coat consists of three
layers. The innermost layer surrounding the cotyledon is spongy and aeriferous. This layer is enclosed in a thin, hard, woody layer. The outermost layer is
thin, smooth, and of a corky texture which tends to obscure the margin of the
woody layer below but usually does not persist.
DISTRIBUTION AND HABITAT
Fevillea cordifolia has the widest distribution, ranging from southern Mexico,
east into the Caribbean to Puerto Rico, south through Central America and into
South America to northern Argentina. Dieterle (1976) notes that it is cultivated
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in some or all Central American countries and is found in most Central American markets, especially in Guatemala. Three species (F. trilobata, F. bahiensis, and
F. passiflora) are endemic to eastern Brazil and F. pedatifolia and F. pergamentacea
occur in Ecuador, Peru, and Bolivia, with F. pedatifolia extending into adjacent
Amazonian Brazil. Fevillea moorei is known only from the type material cultivated in England and is probably from Guyana or Amazonian Brazil.
Fevillea typically occurs along river banks, along the edge of tropical primary or secondary forests, and along the edge of seasonally inundated riverine
forests, occasionally climbing to heights of 35 m in forest canopy openings. It
also is found in forest clearings and along roadsides. It occurs at elevations from
near sea level to about 500 m, less commonly up to 1,700 meters.
Fruits and seeds of Fevillea are quite buoyant and thus apparently are well
suited to dispersal in fresh water. Gentry and Wettach (1986) report that at least
one species (F. cordifolia or F. pedatifolia) of Amazonian Peru occurs in seasonally inundated forests, a habitat in which water dispersal is prevalent. Seed drift
materials of Fevillea cordifolia have been found within the Caribbean basin
well outside the species natural range. Gunn and Dennis (1976), Morton (1981),
and the senior author have identified seeds of F. cordifolia collected from beaches
of southern Florida. Guppy (1917) reported materials found along beaches of
the Turks Islands, Tobago, and Grenada. Guppy (1917) and Gunn and Dennis
(1976) found that seeds of F. cordifolia germinated in fresh water while afloat
after the disintegration of the fruit wall, but were generally rendered non-viable in salt water. Although F. cordifolia is sometimes listed as an estuarine plant,
the seeds are probably not capable of over-sea transport for any distance. However, dispersal by seed drift via salt water can not be disregarded. Guppy (1917)
estimated that 5% of the Fevillea cordifolia drift seeds reaching the Turks Islands were viable while Gunn and Dennis (1976) found 20% of the undamaged
drift seeds on Florida beaches were viable. The high salinity of the beach is
probably lethal, thus preventing colonization.
ECONOMIC IMPORTANCE
The high seed oil content of Fevillea trilobata was recognized centuries ago by
indigenous Brazilians whose use of it was first documented by Marcgrave (Piso
& Marcgrave 1648). Fevillea cordifolia is similarly well known in the ethnobotanical literature (cf. Gentry & Wettach 1986). It has been used as a purgative,
reputed antidote for many kinds of poisoning, and as a treatment for numerous
diseases. In Jamaica it is called “antidote caccoon” or “antidote vine” (Adams
1972; Gunn & Dennis 1976; Morton 1981). Lindley and Moore (1870) first reported the use of Fevillea seeds by Peruvians as candles. Gentry and Wettach
(1986) report that “abiria” (Fevillea pedatifolia) is used as candles by the Campa
Indians of the Pichis Valley of Peru.
Fevillea seeds may have potential as an edible or fuel oil source. Calculated
ROBINSON AND WUNDERLIN, REVISION OF FEVILLEA
1975
on a weight per fruit basis, the seed oil content of Fevillea is higher than that of
any other dicotyledon (Gentry & Wettach 1986). Preliminary analysis of oils
extracted from the seeds of two Peruvian species (F. cordifolia and F. pedatifolia)
by Gentry and Wettach show the oil to be simple triglycerides, slightly heavier
than those of refined cottonseed oil. All species were rich in the saturated lowweight fatty acids, palmitic (21–60%) and stearic (10–42%), and the unsaturated oleic (17–17%) and linoleic (6–7%). When compared with previous results
from the Brazilian F. trilobata (Tulloch & Bergter 1979), Gentry and Wettach
suggest that the Peruvian species with 60–70% low-weight, saturated fatty acids would be a good sources of fuel oil while the Brazilian species with 57%
unsaturated fatty acids would be a good source of polyunsaturated edible oils.
However, the relatively high concentration of high molecular weight fatty acids in F. trilobata, probably correlated with its purgative properties, may reduce
its value as an edible oil. The high percent of stearic acid in F. cordifolia might
also suggest its use in the candle industry where this chemical is used to harden
waxes and in the rubber industry where used as an extender. Preliminary laboratory analysis of F. cordifolia at the University of South Florida gave highly
variable results thought to be related to the different ages of the seeds tested,
further complicating the use of Fevillea seeds as a potential commercial oil
source (unpublished data). Although Fevillea as an oil source is documented
in the literature, to date it remains a genus of little or no economic importance.
INFRAGENERIC RELATIONSHIPS
Jeffrey (1962a) recognized two genera within the subtribe Fevilleinae, Fevillea
and Anisosperma. In our treatment, Anisosperma is reduced to a subgenus of
Fevillea. Subgenus Anisosperma differs from subgenus Fevillea by the shape
of the corolla lobes, the character of the median adaxial glandular ridge of the
staminate petals, the congested staminate inflorescence, the lack of glandular
calycine squamellae on the staminate flowers, and the fruit shape. However,
with the presence of the foliar glands, the median adaxial glandular ridge on
the petals, and overall similarity in fruit and seed morphology, the single species of subgenus Anisosperma is easily accommodated in Fevillea.
Within subgenus Fevillea, three species groups can be distinguished on
the basis of foliar gland characters. The first group consists of F. pergamentacea
and F. pedatifolia which have conspicuous petiolar glands and inconspicuous
laminar glands. The others are characterized by having laminar glands only.
Of these, F. cordifolia and F. trilobata have glands terminating the veins on the
lamina and lack basal laminar glands while F. moorei and F. bahiensis both have
basal laminar glands only.
SYSTEMATIC TREATMENT
Fevillea L., Sp. Pl. 1013. 1753. Nhandiroba Adan., Fam. Pl. 2:139. 1763, nom. illegit.
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TYPE: Fevillea trilobata L. Lectotype designated by M.L. Green (in Sprague et al., Nom. Prop.
Brit. Bot. 190. 1929). This lectotypification replaces the lectotype of Fevillea cordifolia L. of
Britton and P. Wilson. (Sci. Surv. Porto Rico 6:270. 1925) under Art. 10.5b of the St. Louis Code.
Anisosperma Silva Manso, Enum. Subst. Braz. 38. 1836. TYPE: Anisosperma passiflora (Vell.) Silva
Manso [=Fevillea passiflora Vell.].
Hypanthera Silva Manso, Enum. Subst. Braz. 37. 1836. TYPE: Hypanthera guapeva Silva Manso
[=Fevillea trilobata L.].
Dioecious vines or lianas; stems sulcate; tendrils axillary, sulcate, distally 2-fid,
coiling both above and below the bifurcation. Leaves alternate, petiolate, the
blade unlobed, or palmately 3- to 7-lobed, or 3- to 5-foliolate, with glands on
the leaf margins terminating the primary lateral veins and/or 2 glands at the
blade base or on the petiole, the petiole canaliculate, sometimes bearing 2 glands
at or above the middle. Staminate inflorescences paniculate or subumbelliform,
many-flowered, bracteate; flowers short-pedicellate; hypanthium pedicelloid;
calyx lobes 5, fused to the petals above, not completely enclosing the petals in
bud, with a glandular calycine squamella on each calyx lobe at or near the point
of fusion with the petals (except in F. passiflora); petals 5, fused to the sepals
below, the lobes each with a median, adaxial, uncinate, flap-like appendage or
a slightly raised ridge or (in F. passiflora) with a thick, glandular ridge; stamens
5, equal, free, inserted near the center of the flower, the anthers bilocular, extrorse,
dehiscing longitudinally, the connective with an adaxial glandular protuberance or projection; pollen prolate, 18–22 µ in length, tricolporate, coarsely striate.
Pistillate flowers solitary or in pairs; hypanthium deeply cupular; sepals and
petals as in the staminate flowers or sometimes the petals differing in shape;
ovary partly inferior, 3-locular, the styles 3, free, outwardly curved, the stigmas
reniform, capitate, the ovules pendulous, usually 4 in each locule. Fruit globose,
gourd-like with a thick, fleshy rind, zonate above the middle with the hypanthium lip scar or non-zonate, indehiscent or rarely circumscissile dehiscent
along the hypanthium lip scar; seeds large, orbicular, somewhat compressed,
the seed coat consisting of a thick, spongy, aeriferous inner layer surrounded by
a thin woody layer, and an outer, usually non-persistent layer, the lateral surface
smooth or striate-verrucose, the outer edges smooth or tuberculate, the inner
kernel disk-like, oily.
Two subgenera are distinguished as follows:
1. Corolla lobes of the staminate flowers suborbicular, the base cuneate, with a median adaxial uncinate appendage or sharply defined ridge; glandular calycine
squamellae present between the petals and the calyx lobes; staminate flowers in
spreading panicles; fruit subglobose, zonate above the middle, the apex rounded
________________________________________________________________ subg. Fevillea
1. Corolla lobes of staminate flowers oblong-hastate, the base with a median adaxial
glandular ridge broadening downward; glandular calycine squamellae absent;
staminate flowers in congested panicles or subumbelliform; fruit ovoid to oblong,
not zonate, the apex short-apiculate ______________________________ subg. Anisosperma
ROBINSON AND WUNDERLIN, REVISION OF FEVILLEA
1977
Fevillea subgenus Fevillea
Fevillea section Javilla M. Roem., Fam. Nat. Syn. Monogr. 2:116. 1946. TYPE: Fevillea javilla Kunth
[=Fevillea cordifolia L.].
Staminate inflorescences paniculate; glandular calycine squamellae present;
corolla lobes suborbicular with a median adaxial uncinate appendage or slightly
raised ridge. Fruit subglobose, zonate above the middle, the apex rounded.
1. Leaves pedately 3- to 5-foliolate ______________________________________ F. pedatifolia
1. Leaves lobed or unlobed, but not pedately foliolate.
2. Leaf blade without glands at the base or on the petiole, with marginal glands
terminating the veins.
3. Leaf blade with angled or rarely with rounded lobes, the marginal glands
inconspicuous; staminate flowers with the hypanthium densely stipitateglandular pubescent, the pedicel with non-glandular trichomes __________ F. trilobata
3. Leaf blade unlobed or occasionally with rounded lobes, the marginal glands
conspicuous; staminate flowers with the hypanthium and pedicel variously
pubescent but not as above ______________________________________ F. cordifolia
2. Leaf blade with glands at the base or on the petiole, with or without marginal
glands terminating the leaf veins.
4. Leaves with glands only at the blade base, without marginal glands terminating the leaf veins of the blade.
5. Staminate flowers 3–5 mm wide; leaves drying reddish-brown, the blade
with a conspicuous uncinate-ciliate margin _______________________ F. bahiensis
5. Staminate flowers 15–20 mm wide; leaves drying green, the blade with a
smooth margin ________________________________________________ F. moorei
4. Leaves with glands either at the blade base or on the petiole, also with marginal glands terminating the veins of the blade.
6. Leaves with glands at the blade base _______________________ F. pergamentacea
6. Leaves with glands on the petiole ______________________________ F. pedatifolia
Fevillea bahiensis G. Robinson & Wunderlin, sp. nov. (Fig. 1). TYPE: BRAZIL. BAHIA:
8 km to the N of Ubaitaba on BR 101, 16 Jun 1972, dos Santos 2307 (HOLOTYPE: CEPEC; ISOTYPE: K).
Species haec a Fevillea moorei Hook. f. differt floribus staminatis minoribus, foliis in siccitate badiis
usque atrobrunneis marginibus uncinato-ciliatibus.
Vine or liana; stem glabrous to lightly appressed golden brown-pubescent; tendrils glabrous to lightly pubescent. Leaves unlobed, the blade ovate, (2.5–)6.5–
10.5(12) cm long, (3.5–)5.5–9 cm wide, membranaceous, drying dark brown to
reddish brown, 5-nerved, the apex acuminate, the base cordate to truncate, the
margin entire, with two irregularly shaped glands at the base near the petiole,
the upper and lower surfaces glabrous or with scattered, appressed, golden
brown trichomes, these usually denser along the leaf veins, the margin uncinate-ciliate, the petiole (1.5–)3.5–5 cm long, glabrous to lightly pubescent. Staminate flowers in a paniculate inflorescence on reduced subterminal, lateral
branches, the branches subtended by a reduced leaf; pedicel 1.5–2 mm long,
glabrous or sparsely pubescent; bracts linear, ca. 1 mm long; hypanthium 1.5–2
mm long, lightly golden brown-pubescent; calyx shallowly cupular, the lobes
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FIG. 1. Fevillea bahiensis. A. Habit, staminate inflorescence (dos Santos 2307). B. Staminate flower (dos Santos 2307).
up to 1.5 mm long, 1 mm wide, glabrous to sparsely pubescent abaxially, the
margin entire, the apex rounded, with scattered stipitate glands, with a glandular calycine squamella at or near the point of fusion with the petals; petals
suborbicular, 2.5–3 mm long, ca. 1.5 mm wide, cream-colored, the margin entire, the median adaxial ridge slightly raised; stamens 1–1.5 cm long, the anthers ca. 0.25 mm long, slightly longer than wide, the filaments ca. 0.5 mm long.
Pistillate flowers solitary; calyx deeply cupular, the lobes ca. 1.5 mm long, ca. 1
mm wide, dark brown, fleshy; petals strap-shaped, ca. 2 mm long, ca. 1.5 mm
wide, cream-colored. Immature fruit subglobose, 2–4 cm long and wide, the
surface smooth; mature fruit not seen.
Distribution and ecology.—Endemic to Brazil in southern Bahia.
ROBINSON AND WUNDERLIN, REVISION OF FEVILLEA
1979
Additional specimens examined. BRAZIL. Bahia: Nova Esperança, São Lourenço, 32 km W of
Wenceslau Guimarães, 26 Jul 2001, Mattos-Silva et al. 4479 (NY); Ramal da Torre da Embratel, entrance 15 km from the Ubaitabe/Itacaré Road (BR 654), 5.8 km from the entrance, 6 Jun 1978, Mori &
dos Santos 10135 (CEPEC, K, NY); km 3, Uruçuca-Taboquinha highway, 19 Jun 1972, dos Santos 2316
(CEPEC); access road to Torre da Embratel, entrance to the right of road to Ubaitabe/Itacaré (BR
654), 24 Sep 1977, dos Santos 3130 (CEPEC, K); Almadina Mata da Serra Pancadinho, 10 Mar 1971,
Pinheiro 1076 (CEPEC, K).
Fevillea bahiensis is most similar and probably most closely related to Fevillea
moorei of Guyana Amazonian Brazil. Both species have glands only at the base
of the leaf blade. Fevillea bahiensis differs by having smaller staminate flowers (petals 2.5–3 mm long vs. ca. 1 cm long in F. moorei) and the leaves drying a
dark reddish brown and with conspicuous uncinate-ciliate margins.
Fevillea cordifolia L., Sp. Pl. 1013. 1753. (Fig. 2). Fevillea scandens L., Sp. Pl. ed. 2. 1457.
1763, nom. illegit. Nhandiroba scandens Descourt., Fl. Méd. Antilles, index 66 [t. 198]. 1829,
nom. illegit. Nhandiroba cordifolia (L.) Kuntze, Revis. Gen. Pl. 1:257. 1891. Fevillea cordifolia
L. var. typica Stehlé, M. Stehlé, & Quentin, Fl. Guadeloupe 2(3):133. 1949, nom. inadmiss. TYPE:
“Habitat in America Calidiore” (LECTOTYPE: “Nhandiroba,” Plumier, Pl. Amer. 20, t. 27. 1703).
Lectotypified by C. Jeffrey, (in C.E. Jarvis et al., eds. Regnum Veg. 127:47. 1993).
Fevillea hederacea Poir., in Lamarck, Encycl. 4:418. 1798. Fevillea cordifolia [var.] hederacea (Poir.)
Cogn., in Alph. de Candolle & C. de Candolle, Monogr. Phan. 3:943. 1881. TYPE: “On la cultive
au jardin des plantes. Elle est originaire de 1’Amerique (v.s.)” (HOLOTYPE: P?, n.v.).
Fevillea javilla Kunth, in Humboldt, Bonpland, & Kunth, Nov. Gen. Sp. 2:124. 1817. TYPE: COLOMBIA. Bolívar: Turbaco, Humboldt & Bonpland 1403 (HOLOTYPE: P, n.v. [microfiche IDC 6209
39:III. 7]).
Fevillea karstenii Cogn., in Alph. de Candolle & C. de Candolle, Monogr. Phan. 3:943. 1881.
Nhandiroba karstenii (Cogn.) Kuntze, Revis. Gen. Pl. 1:257. 1891. TYPE: VENEZUELA. DISTRITO
FEDERAL: Capaya, near Caracas, Karsten s.n. (HOLOTYPE: W, n.v.; photo ex W: F, MO). The type
sheet contains a mixed collection of F. cordifolia and probably Selysia prunifera (Poepp. &
Endl.) Cogn. The material of the latter in the lower left portion of the sheet is excluded.
Fevillea triloba Sessé & Mociño, Fl. Mexic. ed. 2. 231. 1894. TYPE: MEXICO. n.v.
Siolmatra mexiae Standl., in J.F. Macbride, Publ. Field Mus. Nat. Hist., Bot. Ser. 13(6):329. 1937.
TYPE: PERU. L ORETO: left bank of Río Marañón, above Rancho Indiana, 110 m, 22 Jan 1932,
Mexia 6406 (HOLOTYPE: F; photo ex F: F; ISOTYPES: BM, K, MO, NY, U, US).
Fevillea uncipetala Kuhlm., Arch. Jard. Bot. Rio de Janeiro 4:365. 1925. TYPE: BRAZIL. PARÁ: Rio
Branco de Obidos, Castanhal Grande, 4 Nov 1919, Ducke s.n. (RB 15924) (HOLOTYPE: RB, n.v.;
ISOTYPE: B, destroyed; photograph ex B: F, MO, NY, US).
Vine or liana; stem glabrous or lightly to densely pubescent or tomentose; tendrils glabrous to lightly glandular-pubescent. Leaves with the blade unlobed
or occasionally 3- to 5-lobed, suborbicular to cordate, (4–)7.5–13(–18) cm long,
(2.5–)5–12(–19) cm wide, membranaceous or coriaceous, 5-nerved, the apex
acute, the base cordate to truncate or rarely rounded, the main lateral veins
terminating in small irregularly shaped glands, the upper and lower surfaces
glabrous to densely pubescent, the petiole (2–)3–7 cm long, glabrous or pubescent. Staminate flowers in a paniculate inflorescence on reduced subterminal,
lateral branches, the branches subtended by a glandular bract 0.5–4 mm long;
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FIG. 2. Fevillea cordifolia. A. Habit, staminate inflorescence (Lent 3288). B. Staminate flower (Klug 3090). C. Fruit (Huashikat
1078). D. Seed (Huashikat 1078).
pedicel 2–4 mm long, glabrous to densely pubescent; bracts linear, glandular,
ca. 0.5 mm long; hypanthium 3–4 mm long, glabrous to densely pubescent; calyx shallowly cupular, the lobes 1–2.5 mm long, 1–1.5 mm wide, obtuse or
rounded, densely to sparsely glandular-pubescent, the margin entire, the apex
rounded, with a small glandular calycine squamella protruding from each sepal at or near the point of fusion with the petal; petals suborbicular, 3.5–5 mm
long, 2.5–4 mm wide, white, whitish green, cream-colored, light brown, pink or
pinkish orange, dark red, or reddish purple, the margin undulate, the median,
adaxial ridge with an uncinate appendage; stamens ca. 1 mm long, the anthers
ca. 0.5 mm wide, slightly longer than wide, the filaments ca. 0.5 mm long. Pistillate flowers solitary or in pairs; calyx deeply cupular, the lobes suborbicular,
ROBINSON AND WUNDERLIN, REVISION OF FEVILLEA
1981
ca. 3 mm long and wide, pustulate, fleshy; petals oblong, ca. 5 mm long, ca. 3.5
mm wide, cream-colored, the median adaxial appendage slightly raised, with 2
small suborbicular glands on each side of the ridge at the base. Fruit subglobose,
gourd-like, 10–12 cm in diameter, 10–16 cm long, the surface pustulate, mottled
green, zonate above the middle with the hypanthium lip scar and marked at
the apex by a raised triradiate line; seeds orbicular, compressed, 1–2.5 cm thick,
4–6(–7.5) cm wide, the lateral surface of the woody layer striate-verrucose or
pustulate, with the outer edges smooth or occasionally tuberculate, the tubercles
2–3 mm long.
Distribution and ecology.—Southern Mexico east to Puerto Rico, south
through Central America, and into South America to Bolivia. A canopy plant
of wet forests from sea level to 1,700 meters.
Selected specimens examined. MEXICO. Guerrero: Acapulco, 1894–1895, Palmer 335 (MO). GUATEMALA. Sacatepéquez: near Antigua, 1500–1600 m (cultivated, found in market), Nov 1938–Feb 1939,
Standley 63809 (F). NICARAGUA. Río San Juan: 1 km E of the village of Sábalo, 11°02'N, 84°29'W, 50
m, 6 Sep 1985, Moreno 26249 (MO); between Pueblo de San Juan del Norte Nuevo and La Casa de
Ramón Castillo Viajando by San Juanillo, 10°55'N, 83°49'W, 0–100 m, 7 Jul 1994, Rueda et al. 1839
(MO); Río Pigibaye, 18 Feb 1995, Rueda et al. 3199 (MO); Reserva Indio-Maiz, along Río Indio, 11°06'N,
83°58'W, 5–20 m, 19 Sep 1998, Rueda et al. 8822 (MO). Rivas: Isla Ometepe, Volcán Maderas, Hacienda
“La Argentina,” 11°27'–28'N, 85°31'W, 700–900 m, 15 Jun 1984, Robleto 864 (MO); “Las Cuchillas,” Isla
Ometepe-Volcán Maderas, 11°27'N, 85°28'W, 400–800 m, 2 Jun 1985, Robleto 1972 (MO). Zelaya: Caño
Monte Cristo, “La Grupera,” 11°33'N, 87°48'W, ca. 10 m, 4 Feb 1982, Moreno & Sandino 14743 (MO,
NY). COSTA RICA. Heredia: Finca La Selva, OTS field station on the Río Puerto Viejo just E of its
junction with the Río Sarapiquí, 24 Mar 1980, Hammel 8251 (MO). Limón: Tortuguero-Sierpe basin,
near Río Sierpe and Río Penetencia, 10°32'40"N, 83°32'50"W, 20 m, 21 Jan 1997, Hammel & Grayum
20720 (MO); Río Jiménez, 18 Mar 1973, Lent 3288 (F, MO); Cordillera de Talamanca, Reserva Biológica
Hitoy Cerere, road between Estación de la Reserva and Cerere, 9°40'20"N, 83°01'35"W, 100 m, 23 Feb
1989, Herrera & Chacón 2434 (MO). Puntarenas: Península de Osa, Estación de Oro, along the
Aquaduct, 08°42'00"N, 83°29'10"W, 150 m, 10 Feb 1996, Angulo 517 (MO, NY); Península de Osa, La
Palma, Guadalupe, Finca de Efraín González, 08°38'30"N, 83°28'00"W, 50 m, 17 Aug 1993, Aquilar
2119 (MO); Península de Osa, Rancho Quemado, road to Draque, 08°42'00"N, 83°33'00W, 100 m, 30
Jan 1991, Nielsen 895 (MO); Valle de Coto Colorado, 08°46'00"N, 83°15'00"W, 100 m, 25 Jun 1993,
Quesada & Segura 705 (MO); Playa San Josecito, Península de Osa, 08°37'00"N, 83°44'00"W, 10–100
m, 10 Dec 1993, Quesada et al. 848 (MO); Valle de Coto Colorado, shore of Río Esquinas, mouth of Río
Esquinas, 08°44'00"N, 83°20'00"W, 30 m, 17 Dec 1993, Segura et al. 255 (NY); Forest de Santo Domingo
de Golfo Dulce, Mar 1896, Tonduz 10078 (BR). San José: Cordillera de Talamanca, Las Nubes, Estación
Santa Elena, 09°23'30"N, 83°36'30"W, 1150 m, 14 Feb 1996, Alfaro 477 (MO). PANAMA. Chiriquí: Burica
Peninsula, Rabo de Puerco, 8 km along road W from Puerto Armuelles, 150 m, 19 Feb 1973, Busey 440
(F, MO, NY, USF). Colón: Barro Colorado Island, 100 m S of Zetek Trail, 600 m, 26 Aug 1970, Croat
11918 (F, MO, NY, USF). Darién: Río Sabana, above Sante Fe, 14 Sep 1967, Duke 14107 (MO). Los Santos:
17.8 mi S of Macaracas, ca. 300 m, 25 May 1967, Burch 1605 (MO). Panamá: 12.4 km E of Canita, 10 Oct
1975, Witherspoon 8704 (MO). CUBA. Oriente: Bayate at Río Jagua, 4 May 1919, Ekman 9613 (G, K, NY,
US). JAMAICA. Portland: gorge of the Swift River at Eden, 0.5 mi N of Paradise, ca. 30 m, 19 Mar 1956,
Proctor 11871 (MO). St. Andrew: Hope Gardens, 29 May 1902, Harris 8381 (BM, NY). St. Ann: cave near
St. Ann’s Bay, Dec 1873, Purdie s.n. (K). St. Mary: Wapping Stairs, N side of Guys Hill, 20 Mar 1960,
Proctor 20713 (NY). St. Thomas: near Dove Hall, 10 Feb 1850, Alexander s.n. (K, NY). HAITI. Massif du
Nord, Le Borgne, edge of RiviPre du Borgne, 12 Sep 1925, Ekman 4851 (US). DOMINICAN REPUBLIC.
1982
BRIT.ORG/SIDA 21(4)
El Seibo: Cordillera Oriental, ca. 6–8 km S of Miches-Las Lgunas de Nisibon Highway, on road to
Batey Arroyo Santiago, basin of Río Yeguada (S of Miches), 18°55'N, 69°04'W, 80–100 m, 28 Jun 1990,
Zanoni & Jiménez 44609 (MO). La Vega: Jarabocoa, Monabao, Los Calabazos, Arroyo Frio entrance,
19°4'23"N, 70°43'34.6"W, ca. 774 m, 19 Mar 2001, Ososki & Saborío 299 (NY). PUERTO RICO. Along
road between Utuado and Adjuntas, km 40, 2 Feb 1997, Acevedo & Angell 9419 (NY); Bayamón, 31
Mar 1885, Sintenis 986 (BM, BR, G, K, M, NY, US). COLOMBIA. Amazonas: Loreto-Yacú River, ca. 100
m, Sep 1946, Schultes & Black 83351 (K). Antioquia: near Río León ca. 20–30 km upstream and S of the
river mouth ca. 15 km W of Chigorodó, ca. 7°45'N, 76°50'W, ca. 100 m, 14 Mar 1962, Feddema 1907
(NY) ; Murrí la Blanquita, Río Murrí, 06°35'N, 76°50'W, 960 m, 28 Feb 1992, Gentry et al. 75799 (MO);
km 28.8, Nutibara-La Blanquita road, 06°40'N, 76°27'W, 1020 m, 5 Nov 1988, Zarucchi et al. 7172 (MO).
Atlántico: Barranquilla and vicinity, Jan 1934, Elias 1173 (F, US). Bolívar: vicinity of Turbaco, Nov
1920, Heriberto 469 (F, US). Chocó: Río San Juan, Quebrada del Taparal, 5–20 m, 30 May 1946,
Cuatrecasas 21504 (F); Río Chintado, 1–2 1/2 hrs. above La Nueva, 6 Feb 1967, Duke 9865 (NY); right
bank of Río Baudó, ca. 18.5 km upstream of estuary, between estuary of Quebrada Porquera and the
sawmill Porquera, ca. 5 m, 6 Feb 1967, Fuchs & Zanella 21791 (NY). Cundinamarca: Sierra de Subía, 6.6
km N of Cumaca along road to Viota, 1700 m, 22 Jun 1972, Barclay et al. 3521 (US). Magdalena: Santa
Marta, 5 mi S of Ciénaga, near sea level, 12 Sep 1898–1899, Smith 1607 (BM, BR, F, G, MO, NY, US). Meta:
Serranía de la Macarena, Plaza Bonita, bank of Río Güejar, 400 m, 14 Nov 1949, Philipson et al. 1423 (F,
BM, US). Putamayo: Frontera Colombia-Ecuatoriana, along Río San Miguel, at mouth of the Río Conejo,
300 m, 9 Dec 1940, Cuatrecasas 10915 (US); San Antonio, Alto Campucana path, Finca La mariposa,
1350–1420 m, 01°12'N, 76°38'W, 10 Apr–1 May 1994, Fernández et al. 10745 (NY). Vaupés: Río
Guayabero, 240 m, 8 Nov 1939, Cuatrecasas 7499 (US). VENEZUELA. Apure: Reserva Forestal San
Camilo, vicinity of Chirocoa, 9–10 km E of Caserío San Camilo (El Nula), 200 m, 1 Apr 1968, Steyermark
et al. 101665 (MO, NY). Aragua: Parque Nacional Henri Pittier, Estación Biológica de Rancho Grande,
6 Jun 1987, Rojas & Rojas 3617 (MO, NY); Parque Nacional Henry Pittier, between trail up Periquito
and Fila de Periquito, along upper slopes of tributary to Quebrada Palo Vaco on side towards Lago
Valencia, opposite Rancho Grande Biological Station, 1300–1400 m, 25 Oct 1961, Steyermark 89886
(F, NY, US). Carabobo: Río Morón, E of Morón, 10°17–18'N, 68°10–16'W, 0–50 m, 20–21 Jul 1991, Diaz &
Jiménez 487 (MO). Delta Amacuro: between La Margarita and Puerta Miranda, Río Cure, 80–100 m,
26 Nov 1960, Steyermark 87780 (NY, US); Río Acure, 29 Jan 1980, Trujillo & Sulbaran 16234 (MO).
Distrito Federal: Hacienda Chichiriviche, ca. 300 m, Jul 1958, Aristeguieta 3225 (NY, US). Mérida:
0.5–2 km above dam site on Río Guaimaral, 7°45'N, 71°29'W, 15 Mar 1981, Liesner & González 10637
(MO). Miranda: Carretera Santa Teresa–Guatopo, ca. 300 m, 4 Jun 1959, Trujillo 4149 (US). Yaracuy:
Sierra de Aroa, 2 Jul 1953, Aristeguieta & Pannier 1854 (NY). Zulia: ca. 5 km SSE of Destacamento
Guasare No. 1 (La Yolanda), 10°52'10"N, 72°29'30"W, 250–350 m, 16 Nov 1982, Bunting et al. 12420
(NY); 8 km from San José de Los Altos on road to Caño Colorado, 390 m, 27 Nov 1977, Jeffrey & Trujillo
2396 (F, K, MO); 6 km W of main road and 2 km S of Río Catatumbo, 09°6'N, 72°42'W, ca. 20–100 m,
29 Mar 1982, Liesner & González 13347(MO, NY). ECUADOR. Morona Santiago: El Centro Shuar
Pampants, Río Kankaim (Cangaime), 02°47'S, 77°36'W, 300 m, 10 Sep 1985, Warush RBAE85 (NY).
Napo: 5 km SE of Las Sachas, 300 m, 13 Apr 1985, Baker et al. 5995 (NY); Parroquia Dureno, indigenous Cofán-Dureno community, 00°02'S, 76°42'W, 350 m, 29–31 Dec 1987, Cerón & Cerón 3107 (MO,
NY); Estación Biológica Jatun Sacha, Río Napo, 8 km E of Misahuallí, 01°04'S, 77°36'W, 450 m, 22 Oct
1988, Cerón & Iguago 5510 (MO); Hollín-Loreto-Coca highway, between Avila and Río Pucuno, 00°39'S,
77°22'W, 800 m, 10 Dec 1987, Cerón et al. 2871 (MO, NY); Parque Nacional Yasuní, along Maxus road
and pipeline construction project, km 54–54, 13–16 Sep 1993, Dik 436 (MO, USF); km 2, new CotundoCoca highway, 1130 m, 5 Aug 1984, Dodson et al. 15057 (MO); Coca-Auca oilfields road, km 53, 00°50'S,
76°52'W, 400 m, 20 Aug 1979, Jaramillo & Coello 19710 (NY, US); Maxus road, km 1.8, 00°27'S, 76°38'W,
21 Sep 1997, Klitgaard et al. 617 (NY); Parque Nacional Yasuní, Añangu, along Río Añangu near junction with Río Napo, 0°31'S, 76°23'W, ca. 270 m, 16 Jun 1982, Luteyn et al. 8498 (NY); near NW corner
of Lake Limóncocha, Sep 1969, Mowbray 69951 (MO); along Río Indillama, tributary of Río Napo,
ROBINSON AND WUNDERLIN, REVISION OF FEVILLEA
1983
Comuna Pompeya, 00°30'S, 76°40'W, 220 m, 5 Dec 1992, Neill et al. 10192 (MO, NY); right bank of Río
Napo, 8 km from Puerto Misahuallí, 01°04'S, 77°37'W, 450 m, 7–16 Sep 1988, Palacios 3006 (MO, NY);
Codo Sinclair, 00°08'S, 77°27'W, 650 m, 16–20 Sep 1990, Palacios 5719 (MO); Río Huataraco, towards
Ishpano, 00°44'S, 77°23'W, 700 m, 30 Nov 1992, Palacios 10510 (MO, USF); 6 km N of Shushufindi,
towards Dureno, 0°10'S, 76°40'W, 450 m, 23 Sep 1985, Palacios et al. 829 (MO); Dureno on Río Aguarico,
2 Jul 1966, Pinkley 103 (MO); Yusuní National Park, along Maxus road and pipeline construction
project, km 21, 00°33'S, 76°31'W, 250 m, 24 Jul 1994, Pitman 646 (MO, USF); 20 km N of Coca,
Palmoriente property, 00°20'S, 77°05'W, 250 m, 3–21 Nov 1989, Rubio 332 (MO, NY). Pastaza: ARCO
oil well Villano 2, 01°25'S, 77°20'W, 400 m, 1–18 Dec 1991, Hurtado 2908 (MO); Petro-Cañada highway
under construction, Via Auca, 115 km S of Coca, 5 km S of Río Tigüino, 01°15'S, 76°55'W, 320 m, 1–6
Mar 1989, Zak 4135 (MO). Pichincha: Santo Domingo de los Colorados, 800 m, 10 Aug 1945, Solís 10928
(F). Carchi: Reserva Indígena Awá, Parroquia Tobar Donoso, sector El Baboso, 78°20'W, 00°53'N, 1600
m, 3 Oct 1991, Rubio & Talcuz 295 (MO, USF). PERU. Amazonas: S of Huampami across Río Cenepa,
700–900 m, 27 Dec 1972, Berlin 716 (MO); Río Santiago, Cantón de la Quebrada Caterpiza, 1 km from
community of Caterpiza, 200 m, 11 Sep 1979, Huashicat 552 (MO, USF); Yamayakat Brosque, 04°55'S,
78°19'W, 320 m, 16 Jan 1996, Jaramillo et al. 881 (MO). Huánuco: vicinity of Tingo María Insupte, 670
m, 16 Aug 1961, Schunke 5645 (F, US). Loreto: Flor de Yarina-Río Samiria, 20 Oct 1982, Ayala et al.
3922 (NY); Explorer’s Inn, Río Amazonas near Indiana, 03°30'S, 73°03'W, 130 m, 20 Feb 1988, Gentry
et al. 61736 (MO); Santa Rosa, lower Río Huallaga below Yurimaguas, ca. 135 m, 1–5 Sep 1929, Killip &
Smith 28720 (NY); Balsapuerto, ca. 220 m, May 1933, Klug 3090 (BM, F, G, MO, NY, US); Quebrada de
Tamishaco above Tamishaco, 7 Nov 1978, Rimachi 4046 (MO); Florída, 8 Feb 1980, Rimachi 4856 (NY);
Río Itaya, highway to San Antonio, near Venezia, 90 m, 21 Sep 1994, Rimachi 11120 (NY); Bosque Nacional de Iparía, along the Río Ucayali near Iparía (80 km at the confluence with Río Pachitea), 250–
300 m, 23 Aug 1968, Schunke 2670 (NY); San Antonio, Río Itaya, 04°10'S, 73°20'W, 150 m, 13 Dec 1982,
Vásquez & Jaramillo3597 (MO); Cocha Pastor, Isla Padre, 03°45'S, 76°10'W, 116 m, 21 Dec 1982, Vásquez
et. al. 3683 (NY); Indiana, Explorama Inn, 03°30'S, 73°05'W, 108 m, 12 Apr 1992, Vásquez et al. 18213
(MO). Madre de Dios: Parque Nacional del Manu, Cocha Cashu Biological Station, 21 Aug 1976, Foster
& Augspurger 3394 (K, MO, NY, US); Cocha Cashu Camp, Parque Nacional de Manu, along Río Manu,
380 m, 22 Oct 1979, Gentry et al. 27161 (NY); Cuzco Amazónico Lodge, 15 km NE of Puerto Maldonado,
12°35'S, 69°03'W, 200 m, 18 Jun 1990, Núñez 12192 (MO); Las Piedras, Cusco Amazónico, Río Madre de
Dios, 12°29'S, 69°03'W, 200 m, 13 Aug 1991, Timaná 1997 (MO). San Martín: Valley of San Martín, E of
Tarapoto, Funde de San Isidro near Codo Creek, 1000 m, 15 Aug 1937, Belshaw 3230 (NY); Pongo de
Cainarachi, Río Cainarachi, tributary of Río Huallaga, ca. 230 m, Sep–Oct 1932, Klug 2749 (BM, F, G,
MO, NY, US); Rioja-Pomacochas road, below Venceremos, ca. 20 km NW of Rioja, 05°45'S, 77°38'W,
1600 m, 8 Feb 1984, Gentry & Smith 45128 (MO); above Chazuta, W of Quebrada Chazuta, 06°34'S,
76°12'W, 200–300 m, 28 Aug 1986, Knapp 8177 (NY); W of Nueva Aspusana (2 hrs down Río Huallaga
from La Roca), 8 Aug 1962, Mathias & Taylor 6116 (MO); Fundo La Campiña, 2 km below Tocache
Nuevo, right bank of Río Huallaga, ca. 400 m, 23 Aug 1969, Schunke 3377 (NY); Tananta (left bank of
Río Huallaga), 6 Oct 1970, Schunke 4479 (NY); Nueva Unión below Puerto Huicte (right bank of Río
Huallaga), 450–500 m, 1 Aug 1974, Schunke 7965 (NY). Ucayali: Bosque Nacional de Iparía, along the
Río Ucayali near the village of Iparía (ca. 80 km above the confluence with Río Pachitea), 200–300
m, 23 Aug 1968, Schunke 2670 (F, G); Río Novia, right bank at native community San José, 10°12'S,
70°57'W, 189 m, 26 Feb 2002, Schunke & Graham S14909 (NY). BRAZIL. Acre: margin of Rio Azul, ca.
07°29'S, 73°39'W, 13 Oct 1986, Campbell et al. 8995 (NY); Sena Madureira, 28 Sep 1980, Cid & Nelson
2596 (NY); basin of Rio Juruá. right bank of Rio Tarauacá, 8°32'51"S, 71°28'39"W, 17 Nov 1995, Daly et
al. 8562 (MO, NY); near mouth of Rio Macauã (tributary of Rio Iaco), 9°20'S, 69°W, 23 Aug 1933, Krukoff
5610 (BM, F, G, M, MO, US). Amazonas: near mouth of Rio Embira (tributary of Rio Tarauacá), 7°30'S,
70°15'W, 6 Jul 1933, Krukoff 5209 (BM, F, G, M, MO, NY, US). Pará: Belém, 20 Dec 1950, Black 50-10925
(NY); Rio Pacajá 2°50'S, 50°50'W, 15 Oct 1965, Prance et al. 1636 (NY); Rio Mocoões, 45 min. below
Frances, 00°45'S, 49°41'W, 10 Nov 1987, Prance et al. 30399 (MO, NY); Altamira, left bank of lower
1984
BRIT.ORG/SIDA 21(4)
Rio Xingu, 19 Oct 1986, Souza et al. 385 (NY); Travessão do CNEC, between D13 and edge of Rio Xingu,
2 Dec 1986, Souza et al. 635 (NY); Ilha de Marajó, Cuantã, above Anajás, Rio Anajás, 00°57'S, 49–48°W,
2 Nov 1987, Tavares 334 (NY). Rondônia: E bank of Rio Madeira at Misericórdia between Cachoeiras
Misericórdia and Madeira, 30 Jul 1968, Prance et al. 6620 (NY). BOLIVIA. Cochabamba: Proyecto Valle
del Sacta, km 240 on Santa Cruz-Villa Tunari highway, 17°00'S, 64°46'W, 290 m, 12–14 Jul 1989, Smith
et al. 13711 (MO). El Beni: Río Beni, above confluence with Río Quiquibey, 3.5 hrs. upstream from
Rurrenabaque, 14°44'S, 67°25'W. 320 m, 23 May 1990, Daly et al. 6590 (MO, NY). La Paz: Parque Nacional Madidi, 10.2 km NW of turnoff in Tumupasa, 200–500 km from summit, 14°09'57"S, 67°55'02"W,
830 m, 9 Aug 2000, Croat et al. 84416 (MO); Santa Fe, NE of community,13°40'S, 68°12'W, 250 m, 10
Aug 1995, DeWalt et al. 823 (MO, NY); basin of Río Bopi, San Bartolomé near Calisaya, 750–900 m, 1–
22 Jul 1939, Krukoff 10528 (F, G, K, MO, NY, US); Parque Nacional Madidi, near Arroyo Aguapolo and
Río Tuichi, 270 m, 16 Mar 2002, Macía et al. 6850 (NY). Santa Cruz: Parque Nacional Amboró, along
Río Isamá [“Río Pitasamá”], 17°42–43'S, 63°37–38'W, 475 m, 11 Oct 1990, Nee 39252 (NY); Estancia San
Rafael de Amboró, 15 km (by air) SSE of Buena Vista, 17°35'S, 63°37'W, 375 m, 28 Jul 1987, Nee et al.
35391 (NY); Río Palometilla, 400 m, 16 Jun 1927, Steinbach 7904 (F, G, MO, NY, BM).
Fevillea cordifolia is a polymorphic species exhibiting considerable variation
throughout its range. The species can be readily distinguished from other members of the genus by its conspicuous marginal laminar glands. It is most similar
to F. trilobata of eastern Brazil and is distinguished from that species by the
typically rounded leaf lobes (when lobes are present), rather than the angular
lobes characteristic of F. trilobata. Fevillea trilobata also has a distinctive stipitate-glandular pubescence on the hypanthium of the staminate flowers, which
is sharply differentiated from the uncinate pubescence of pedicel. This pattern
of pubescence is lacking in F. cordifolia.
Fevillea moorei Hook. f., Bot. Mag. t. 6356. 1878. Nhandiroba moorei (Hook. f.) Kuntze,
Revis. Gen. Pl. 1:257. 1891. TYPE: GUYANA or BRAZIL: Cultivated at Liverpool Botanic Garden,
1871, Tyreman s.n. (HOLOTYPE: K; ISOTYPE: BR-fragment).
Vine or liana; stem glabrous; tendrils glabrous. Leaves with the blade unlobed,
broadly ovate, 6–12 cm long, 3.5–7 cm wide, membranaceous, drying light green,
3-nerved, the apex acuminate, the base rounded, with 2 small, irregularly shaped
glands near the petiole, the upper and lower surfaces glabrous, the petiole 1–2.5
cm long, glabrous. Staminate flowers in a racemose inflorescence ca. 6 cm long,
(10–12 cm fide Hooker f.); pedicel 1–4 mm long, glabrous; hypanthium 5–6 mm
long, glabrous; bracts linear, ca. 0.5 mm long; calyx shallowly cupular, the lobes
oblong, ca. 6 mm long, 4 mm wide, the apex obtuse, the margin entire, with a
glandular calycine squamella protruding at or near the point of fusion with
the petals; petals suborbicular, somewhat broader at the apex, ca. 1 cm long, 1
cm wide, pale brick-red, the margin undulate; stamens ca. 4 mm long, the anthers ca. 1 mm long, slightly longer than wide, the filament ca. 3 mm long. Pistillate flowers and fruit not seen.
Distribution and ecology.—Known only from the type material received by
J.D. Hooker from David Moore, curator of the Glasnevin Botanic Garden, Dublin, Ireland, who received it from Mr. Tyreman of the Liverpool Botanic Garden.
ROBINSON AND WUNDERLIN, REVISION OF FEVILLEA
1985
The material was labeled as “Strychnos curari” and said to have come from
Gambia. As suggested by Hooker in the protologue, it is probable that the plant
is from South America, possibly Guyana or the Amazon River basin of Brazil
where Strychnos toxifera, the source of the drug curare is native and was known
to occur at that time. Hooker named the plant in honor of his friend, Dr. Moore.
Fevillea moorei is most similar to F. bahiensis of southern Bahia, Brazil. It
is easily distinguished by its larger staminate flowers, its leaf margins lacking
uncinate trichomes, and its 3-nerved leaves which dry to a light green color.
Fevillea pedatifolia (Cogn.) C. Jeffrey, Kew Bull. 16:199 1962. (Fig. 3).
Alsomitra
pedatifolia Cogn., in Martius, Fl. Bras. 6(4):116. 1878. Siolmatra pedatifolia (Cogn.) Cogn., in
Engler, Pflanzenr. 4(Heft 66):30. 1916. TYPE: BRAZIL. AMAZONAS: Rio Solimões, 1819–1820,
Martius s.n. (HOLOTYPE: M; photo ex M: F, MO, NY, US; ISOTYPES: BR-fragment).
Alsomitra peruviana Huber, Bol. Mus. Paraense Hist. Nat. 4:616. 1908. Siolmatra peruviana (Huber) Cogn., in Engler, Pflanzenr. 4(Heft 66):30. 1916. Fevillea peruviana (Huber) C. Jeffrey,
Kew Bull. 16:200. 1962. TYPE: PERU. UCAYALI: Río Ucayali, near Canchahuaya, 28 Oct 1898,
Huber 1390 (HOLOTYPE: MG, n.v.; photo ex MG: F; ISOTYPE: F-fragment).
Siolmatra amazonica Cogn., in Engler, Pflanzenr. 4(Heft 66):30. 1916. Fevillea amazonica (Cogn.)
C. Jeffrey, Kew Bull. 16:199. 1962. TYPE: BRAZIL. AMAZONAS: Rio Juruá, Juruá Miry, Oct 1901,
Ule 5819 (LECTOTYPE: here designated, K; ISOLECTOTYPES: F-fragment, MG, n.v.; photo ex MG: F;
B, destroyed; photo ex B: F, MO, NY, US).
Siolmatra simplicifolia Harms, Notizbl. Bot Gart. Berlin-Dahlem 11:769. 1933. Fevillea simplicifolia
(Harms) C. Jeffrey, Kew Bull. 16:200. 1962. T YPE : PERU. L ORETO : Lower Río Huallaga,
Yurimaguas, Puerto Arturo, 15 Nov 1929, Williams 5072 (HOLOTYPE: B, destroyed; LECTOTYPE:
here designated, F; ISOLECTOTYPE: US).
Vine or liana; stem glabrous to densely glandular-pubescent; tendrils sparsely
pubescent or glabrous. Leaves with the blade unlobed, or 3- to 5-lobed, or 3- to
5-foliolate, membranaceous to coriaceous, the unlobed or the lobed leaves ovate
to ovate-oblong, (6–)8–15(–18) cm long, 9–14(–17.5) cm wide, 5- to 7-nerved, the
divisions of the lobed leaves or the leaflets of the foliolate leaves (6–)8–15(–18)
cm long, 4–8 cm wide, 1- to 2-nerved, with a petiolule up to 2 cm long, the apex
of the blade or leaf divisions acuminate, the base of the blade or leaf divisions
oblique or rounded, the margin entire or coarsely crenate-toothed, the primary
lateral veins terminating in a small irregularly shaped marginal gland, the upper and lower surfaces glabrous or lightly pubescent, especially along the leaf
veins, the petiole 3.5–5(–7) cm long, glabrous to sparsely pubescent, with 2 opposite, prominent, irregularly shaped median to subapical glands. Staminate
flowers in a paniculate inflorescence on reduced lateral branches, each branch
subtended by a thin scale-like glandular-pubescent bract 0.5–2 mm long;
pedicel 0.5–1 mm long, sparsely glandular-pubescent to glabrate; hypanthium
0.5–1.5 mm long, sparsely glandular-pubescent to glabrate; calyx shallowly
cupular, the lobes light green or greenish brown, suborbicular, 0.5–1 mm long
and wide, the apex rounded or obtuse, glandular-pubescent or glabrous, the
margin slightly erose and glandular-ciliate, with a glandular calycine squamella
1986
BRIT.ORG/SIDA 21(4)
FIG. 3. Fevillea pedatifolia. A. Habit, staminate inflorescence (Klug 4187). B. Staminate flower (Klug 2678). C. Fruit
(Barbour 5533). D. Seed (Barbour 5533).
protruding at or near the point of fusion with the petals; petals suborbicular, 1–
2 mm long, 1–1.5 mm wide, white or greenish white, greenish yellow, or yellowish, the margin slightly erose, the median adaxial ridge slightly raised; stamens
0.25– 0.5 mm long, the anthers ca. 0.25 mm long, slightly longer than wide, the
filament ca. 0.5 mm long. Pistillate flowers in pairs; pedicel 1.2–2 mm long; calyx deeply cupular, the lobes ca. 3 mm long, ca. 2 mm wide, dark greenish brown,
the surface pustulate; petals white. Fruit subglobose, ca. 14 cm long, 13 cm wide,
gourd-like, indehiscent or rarely circumscissile dehiscent along the hypanthium lip scar (A. Gentry, pers, comm.), the surface smooth or pustulate,
usually a mottled green color; seeds orbicular, compressed, 4–5 cm long and
ROBINSON AND WUNDERLIN, REVISION OF FEVILLEA
1987
wide, 1.5–2.5 cm thick, silver-white upon drying, the woody layer smooth to
slightly pustulate, the winged margin ca. 0.5 cm wide.
Distribution and ecology.—Amazonian Ecuador and Peru, south to Bolivia,
and east to Acre and Amazonas, Brazil. A plant of moist to wet forests, occurring at 130–800 meters in elevation.
Selected specimens examined. ECUADOR. Napo: Estación Biológica Jatun Sacha, 8 km E of Misahuallí,
01°04'S, 77°36'W, 400 m 23–31 Jan 1989, Cerón 6076 (MO); km 2, new road from Cotundo to Coca,
1130 m, 5 Aug 1984, Dodson et al. 15072 (NY). PERU. Amazonas: 1 km from La Poza, W of Río Santiago,
180 m, 21 Aug 1979, Huashikat 111 (MO); valley of Río Santiago, Quebrada Caterpiza, 2–3 km behind
the community of Caterpiza, 3°50'S, 77°40'W, 200 m, 8 Feb 1980, Tunqui 783 (MO). Ayachucho: between Santa Rosa and Hacienda Luisiana, 640 m, 9 Sep 1976, Wasshausen & Encarnación 632 (NY).
Huánuco: Codo de Puzuzo, floodplain of Río Puzuzo, S of settlement to main river, 9°40'S, 75°25'W,
450 m, 21 Oct 1982, Foster 9370 (USF). Junín: Río Negro, 800 m, 14 Aug 1960, Woytkowski 5795 (G,
MO, US). Loreto: Yanamono, Explorama Tourist Camp on Río Amazonas between Indiana and mouth
of Río Napo, 03°28'S, 72°48'W, 120 m, 26 Jul 1980, Gentry et al. 29043 (MO); Yanamono, Explorama
Tourist Camp, Río Amazonas halfway between Indiana and mouth of Río Napo, 03°28'S, 72°50'W,
130 m, 13 Jul 1983, Gentry et al. 42937A (MO); Balsapuerto, 220 m, Feb 1933, Klug 2896 (BM, F, G, MO,
NY, US); Indiana, Reserva Explorama (Yanamono), 03°30'S, 72°50'W, 90 m, 28 Sep 1990, Pipoly et al.
12592 (MO); Yanamono tourist camp, 50 mi. NE of Iquitos, 3°30'S, 72°50', ca. 106 m, 19 Oct 1980, Vásquez
& Jaramillo 586 (NY); Indiana, Iquique, 03°30'S, 72°58'W, 115 m, 16 Dec 1987, Vásquez & Jaramillo
10164 (MO); Indiana, Explorama Reserve, 03°28'S, 72°50'W, 106 m, 9 Nov 1989, Vásquez & Jaramillo
13140 (MO). Madre de Dios: Tambopata, 12°50'S, 69°17'W, 260 m, 8 Nov 1988, Alexiades et al. 81 (MO,
NY); Río Piedras, near confluence with Río Pariamanu, 12°40'S, 69°17'W, 260 m, 11 Jan 1991, Alexiades
et al. 1071 (NY); Lago Tres Chimbadas, ca. 65–70 river km SSW of Puerto Maldonado, ca. 10–15 air km
NW effluence of Río La Torre (Río D’Orbigny) Río Tambopata, 12°49'S, 69°17'W, ca. 260 m, 7 Jun
1980, Barbour 5533 (MO); Río Manu, Cocha Cashu Biologial Station, 350 m, 1 Oct 1980, Foster 5439
(NY); Cocha Cashu, vicinity of ox-bow lake of Río Manu, between Panaqua and Tayakome, 17–24
Aug 1974, Foster et al. 3492 (K, MO, US). Las Piedras, Cusco Amazónico, 12°29'S, 69°03'W, 200 m, 24
Jun 1991, Timaná 1844 (MO). Pasco: Río Pichis, 1 hr. below Puerto Bermudez, between Puerto Bermedez
and Paujil, 10°10'S, 74°50'W, 200 m, 17 Jun 1983, Gentry et al. 42148 (MO); Iscozacín, near confluence
of Río Palcazu and Río Iscozacín, 10°12'S, 75°13'W, 430 m, 16 Jun 1982, Smith 1911 (NY); Palcazu Valley,
Río Chuchurras drainage, 10°09'S, 75°20'W, 400 m, 13 May 1983, Smith 4009 (MO, US). San Martín:
Pongo de Cainarachi, Río Cainarachi, tributary of Río Huallaga, 230 m, Sep-Oct 1932, Klug 2755 (BM,
F, G, K, MO, NY, US); Quebrada Cachiyacu de Huaquisha, ca. 500–650 m, 7 Dec 1980, Schunke 12451
(NY). Ucayali: Bosque Nacional von Humboldt, Pucallpa-Tingo María Road, 8°40'S, 75°0'W, 250 m, 13
Feb 1981, Gentry et al. 31307 (MO, USF). BRAZIL. Acre: N bank of Rio Juruá opposite Cruzeiro do Sul,
27 Oct 1966, Prance et al. 2936 (K, MO, NY, US). Amazonas: near Palmares, 11 Sep 26–Oct 1936, Krukoff
8475 (BM, BR, F, G, K, MO, NY, US). BOLIVIA. La Paz: basin of Río Bopi, Asunta (near Evenay), 690–
750 m, 27–31 Jul 1939, Krukoff 10666 (F, G, K, MO, NY).
Plants with 3- to 7-foliolate leaves are easily distinguished from other species of
Fevillea. They previously had been considered a species of Siolmatra because
of this feature, but the presence of the foliar glands, the bilocular anthers, and
the large globose fruit with large unwinged seeds clearly separates it. Siolmatra,
in contrast, lacks foliar glands, has unilocular anthers, and has a cylindric fruit
with winged seeds.
Fevillea peruviana and F. amazonica were separated from F. pedatifolia on
the basis of leaflet number (3 rather than 5). Fevillea amazonica was further
1988
BRIT.ORG/SIDA 21(4)
separated on the basis of the petiolar gland position (median rather than subapical). These characters are not constant and thus F. peruviana and F.
amazonica are here reduced to synonymy as suggested by Jeffrey (1962b).
Plants with unlobed leaves have been called F. simplicifolia. Since specimens with leaves intermediate between simple and 3-foliolate are occasionally
found (although rare) and there are otherwise no other floral or vegetative differences, F. simplicifolia is here reduced to synonomy. Plants with unlobed leaves
are sometimes confused with F. pergamentacea. However that species is readily
distinguished by the presence of a pair of glands at the base of the blade, while
the glands in F. pedatifolia are on the petiole.
Fevillea pergamentacea (Kuntze) Cogn., in Engler, Pflanzenr. 4(Heft 66):8. 1916.
(Fig. 4). Nhandiroba pergamentacea Kuntze, Revis. Gen. Pl. 3(2):104. 1898. TYPE: BOLIVIA.
SANTA CRUZ: Río Yapacaní, 400 m, Jun 1892, Kuntze s.n. (LECTOTYPE: here designated, NY;
ISOLECTOTYPES: NY, B, destroyed; photo ex B: F, MO, NY, US).
Nhandiroba harmsii Kuntze, Revis. Gen. Pl. 3(2):103. 1898. Fevillea harmsii (Kuntze) K. Schum.,
Just’s Bot. Jahresber. 26:383. 1898. TYPE: BOLIVIA. SANTA CRUZ: Velasco, 200 m, Jul 1892, Kuntze
s.n. (LECTOTYPE: here designated, NY; ISOLECTOTYPES: US, B, destroyed; photo ex B; F, MO, NY,
US).
Vine or liana; stem glabrous to lightly pubescent; tendrils glabrous. Leaves with
the blade unlobed or occasionally 2- to 3- lobed, ovate, 10–11(–15) cm long, (4–)
6–8(–15) cm wide, subcoriaceous, drying very light brown or green, the apex or
the lobe tips acuminate or acute to slightly rounded, the base cordate to truncate, the upper surface glabrous, the lower surface lightly pubescent along the
veins, the margin entire, occasionally with scattered trichomes, the lateral veins
occasionally terminating with a small gland, with 2 small, opposite, irregularly auriculate glands at the base of the blade, the petiole 2.5–4 cm long, glabrous to sparsely pubescent. Staminate flowers in a paniculate inflorescence
on reduced lateral branches; pedicel 1–2 mm long, densely to sparsely pubescent; hypanthium 0.5–1 mm long, glabrous; calyx crateriform, the lobes lanceolate, 0.5–1 mm long, ca. 0.5 mm wide, obtuse, slightly erose-margined,
sparsely to densely pubescent, with a prominent glandular calycine squamella
protruding from each sepal at or near the point of fusion with the petals; petals
narrowly obovate, 2–2.5 mm long, 1.5–2 mm wide, cream to yellowish brown,
the margin entire, the median appendage slightly raised; stamens ca. 0.5 mm
long, the anthers ca. 0.25 mm wide, slightly longer than wide. Pistillate flowers
not seen. Fruit globose, 6–7 cm long and wide, green, the surface minutely pustulate; seeds orbicular, compressed, 1.5 cm thick, 3.5–4.5 cm long and wide, the
lateral surface of the woody layer smooth to minutely pustulate, the marginal
nerve ca. 0.5 cm wide, completely enclosing the seed.
Distribution and ecology.—Amazonian Colombia, Ecuador, eastern Peru,
and central Bolivia. A plant of wet forests, occurring between 180 and 500 meters.
ROBINSON AND WUNDERLIN, REVISION OF FEVILLEA
1989
FIG. 4. Fevillea pergamentacea. A. Habit, staminate inflorescence (Klug 2198). B. Staminate flower (Klug 2198).
Additional specimens examined. COLOMBIA. Guaviare: Vereda Miraflores, 02°19'N, 72°26'W, 300 m,
27 Jan 1990, Marulanda & Márquez 1766 (MO). Putamayo: Vereda “La Kofania,” 1°1'N, 77°17'W, 500–
700 m, 2 Sept 1993, Cogollo et al. 6839 (MO). ECUADOR. Napo: Yasuní Forest Reserve, along road from
PUCE Scientific Station to end of road towards Waoroni Territory, 00°40.901'S, 76°24.348'W, 240–
310 m, 29 Jun 1995, Acevedo & Cedeno 7571 (NY); Río Eno NE of Shushufindi, ca. 00°10'S, 76°40'W,
300 m, 11 Apr 1982, Balslev 2321 (NY); Estación Biológica Jatun Sacha, 8 km E of Misahuallí, 01°04'S,
77°36'W, 400 m, 23–31 Jan 1989, Cerón 6076 (MO, NY); Estación Biológica Jatun Sacha, Río Napo, 8
km E of Misahuallí, 01°04'S, 77°36'W, 400 m, 10 Aug 1989, Cerón 7379 (MO, NY); Hollín-Loreto highway, between Avila and Loreto, Huiruno (Quichua community), 00°43'S, 77°19'W, 450 m, 29 Nov
1982, Cerón 7853 (MO); km 2, new Cotundo-Coca highway, 1130 m, 5 Aug 1984, Dodson et al. 15072
(MO, US); Pompeya, S of Río Napo, Río Jivino, Maxus highway, km 1–5, 00°25'S, 76°37'W, 220 m, 23–29
Nov 1992, Grijalva et al. 231B (MO); E of the mission in Ahuano on Río Napo, 550 m, 15 Feb 1973,
Humbles 6214 (F, MO); Yasuní National Park, Río Indillama, small southern tributary of Río Napo,
Comuna Pompeya, 00°30'S, 76°40'W, 220 m, 26 Aug 1992, Neill & Gudiño 10120 (MO, NY); S of Volcán
Sumaco, Hollín-Loreto highway, km 31, Comuna Challua Yacu, 00°43'S, 77°40'W, 1200 m, 20–25 Mar
1989, Palacios 4102 (MO); Río Aguarico, Shushufindi, 244 m, 14 Feb 1975, Vickers 116 (F). PERU. Loreto:
1990
BRIT.ORG/SIDA 21(4)
Florida, Río Putamayo, at mouth of Río Yubineto, 180 m, May–Jul 1931, Klug 2198 (BM, F, G, K, MO, NY,
US). BOLIVIA. Cochabamba: Cochabamba, Bang 1264 (BM, K, MO). El Beni: Trinidad, 164 km towards
Santa Cruz, 28 Aug 1985, Beck 12212 (NY). Santa Cruz: km 11, Río Tres Quebradas road, 14 Aug 1991,
Acevedo et al. 4598 (NY); border of Río Piraí, along Montero-Portachuelo road, 1994, Mostacedo 2288
(NY); 12 km SE of Comunidad Don Lorenzo, 0.5 km E of Estancia Caracore, W side of Río Grande,
17°51'S, 62°47'W, 300 m, 17 Nov 1990, Nee 39986 (MO, NY); Parque Nacional Amboró, 0–2 km SW of
El Carmen, along trail to Quebrada Yapoje and Río Saguayo, 17°32'S, 63°42'W, 360 m, 15 Jun 1991, Nee
41079 (NY); Parque Nacional Amboró, 1–2 km NE of El Carmen on trail to crossing of Río Surutu,
17°31'S, 63°41'W, 350 m, 21 Jul 1991, Nee 41796 (MO, NY); along Quebrada Salada and oil pipeline, first
rocky foothills of the Andes, 4 km W of highway bridge over Río Piraí, 18°06'S, 63°30'W, 750 m, 11
Dec 1991, Nee 42017 (MO, NY); 2 km (by air) NW of center of Bermejo, around Laguna Volcán, 18°07'S,
63°39'W, 1125–1175 m, 24 Dec 1994, Nee 46129 (MO, NY); Parque Nacional Amboró, along Río Verde,
1 km E of Campamento Mataracú, 17°33'S, 63°52'W, 375 m, 31 May 1998, Nee & Bohs 49540 (NY); 4 km
(by air) NE of Bermejo, valley of “Rufugios Los Volcanes,” 18°06.3'S, 63°36'W, 1070–1150 m, 29 Jul 2003,
Nee 52385 (NY); Estancia San Rafael de Amboró, 15 km SSE of Buena Vista, 17°35'S, 63°37'W, 375 m,
30 Jul 1987, Nee & Saldias 35454 (NY, USF); Parque Nacional Amboró, 0.5 km upstream from the last
Andean foothills, 17°40'S, 63°43'30"W, 450 m, 20 Dec 1988, Nee & Saldias 37265 (NY); Río Piray, 450
m, 19 Jul 1924, Steinbach 6259 (G, K); Parque Nacional Amboró, before Río Saguayo, 5 km SW of El
Carmen, ca. 17°33'S, 63°44'W, 400 m, 15–22 Nov 1991, Vargas et al. 1225 (MO, NY); Reserva de Vida
Silvestre Ríos Blanco y Negro, Río Negro de Caimanes, ca. 4 km SE of Río San Pablo, 14°45'07"S, 63°56'W,
250 m, 18 Jun 1993, Vargas 2605 (MO, NY); Reserva de Vida Silvestre Ríos Blanco y Negro, 5 km from
meeting of Ríos San Pablo and Negro de Caimanes, 14°48'05"S, 63°58'W, 200 m, 18–20 Jun 1993, Vargas
2623 (NY).
Fevillea pergamentacea is most similar to simple-leaved forms of F. pedatifolia,
but differs in the position and form of its foliar glands and in the shape of the
staminate flowers. Fevillea pergamentacea is characterized by flat, elongateelliptic glands at the base of the leaf blade rather than petiolar glands well below the base of the leaf blade as in F. pedatifolia. Fevillea pergamentacea also
has a distinctive crateriform staminate flower as opposed to the shallow cupshaped flowers of F. pedatifolia. The distinction between F. pergamentacea and
F. harmsii on the basis of the leaf shape cannot be maintained and F. harmsii is
here reduced to synonymy as suggested by Jeffrey (1962b).
Fevillea trilobata L., Sp. Pl. 1014. 1753. (Fig. 5). Fevillea marcgravii Guib., Hist. Nat. Drog.
Simpl. ed. 4. 3:244. 1850, nom. illegit. Nhandiroba trilobata (L.) Kuntze, Revis, Gen. Pl. 1:257.
1891. TYPE: BRAZIL: (LECTOTYPE: here designated, Marcgrave, in Piso & Marcgrave, Hist. Nat.
Bras. 2:46, unnumbered pl, 1648).
Fevillea cordifolia Vell., Fl. Flumin., Icon. 10:t. 102. 1831 (“1827”); non L., 1753. Fevillea triangularis M. Roem., Fam. Nat. Syn. Monogr. 2:114. 1846. TYPE: BRAZIL. RIO DE JANEIRO: (LECTOTYPE:
here designated, Vellozo, Fl. Flumin., Icon. 10:t. 102. 1831 (“1827”)).
Hypanthera guapeva Silva Manso, Enum. Subst. Braz. 38. 1836. TYPE: BRAZIL. SÃO PAULO: São
Ignácio (n.v.).
Fevillea tomentosa Gardner, London J. Bot. 2:355. 1843. Fevillea trilobata var. tomentosa (Gardner) Cogn., in Martius, Fl. Bras. 6(4):118. 1878. TYPE: BRAZIL. RIO DE JANEIRO: Serra dos Orgãos,
s.d., Gardner 425 (HOLOTYPE: BM; ISOTYPES: G, K; photo ex G: F, MO, US).
Fevillea albiflora Cogn., in Martius, Fl. Bras. 6(4):118. 1878. Nhandiroba albiflora (Cogn.) Kuntze,
Revis. Gen. Pl. 1:257. 1891. TYPE: BRAZIL. BAHIA: without precise locality, s.d., Blanchet 2380
(LECTOTYPE: here designated, G; ISOLECTOTYPES: BR, G, K, NY). SYNTYPE MATERIAL: BRAZIL.
ROBINSON AND WUNDERLIN, REVISION OF FEVILLEA
1991
FIG. 5. Fevillea trilobata. A. Habit, staminate inflorescence (Saint-Hilaire s.n. [Glaziou 87201]). B. Staminate flower (SaintHilaire s.n. [Glaziou 8720]).
1992
BRIT.ORG/SIDA 21(4)
MINAS GERAIS: near Contendas, 1818, Martius 1581 (M); near Contendas, s.d., Saint-Hilaire s.n.
(BR, F).
Fevillea albiflora var. glaziovii Cogn., Bull. Acad. Roy. Sci. Belgique, ser. 3. 14:364. 1887. TYPE: BRAZIL. MINAS GERAIS: Serra do Inficionado, near Caracas, 6 Sep 1882, Glaziou 13906 (LECTOTYPE:
here designated, BR; ISOLECTOTYPES: B, destroyed, K, NY; photo ex B; F, MO, NY, US).
Fevillea trilobata var. longipedicellata Cogn., in Martius, Fl. Bras. 6(4):118. 1878. TYPE: BRAZIL.
RIO DE J ANEIRO: near Copacabana, s.d., Riedel [et Langsdorff, fide Cogn. (1881)] 706 (LECTOTYPE:
here designated, BR; ISOLECTOTYPES: K, M). S YNTYPE MATERIAL: BRAZIL. RIO DE JANEIRO :
Copacabana, Dec 1840, Gardner 5469 (BM); Copacabana, Lund 213 (n.v.); s.d., Sello s.n. (BM).
Fevillea trilobata var. subintegrifolia Cogn., in Martius, Fl. Bras. 6(4):118. 1878. TYPE: BRAZIL. RIO
DE J ANEIRO: Copacabana, s.d., Luschnath 552 (LECTOTYPE: here designated: BR). SYNTYPE MATERIAL: BRAZIL. RIO DE JANEIRO: Copacabana, Luschnath 950 (n.v.); Blanchet 955 (n.v.).
Fevillea trilobata var. subuniflora Cogn., in Martius, Fl. Bras. 6(4):118. TYPE: BRAZIL. RIO DE JANEIRO: Gávea, Glaziou 3986 (n.v.).
Vine or liana; stem densely pubescent, tomentose to lightly pubescent, or
subglabrous; tendrils pubescent or glabrous. Leaves with the blade 3-lobed, or
occasionally 5-lobed, 6–10 cm long, (2–)5–10(–15) cm wide, membranaceous,
the apex acute or acuminate, the main lateral veins occasionally terminating
in a small apical gland, the upper and lower surfaces densely to lightly pubescent. Staminate flowers in a paniculate inflorescence on reduced lateral
branches; pedicel with uncinate trichomes, 1–3(5) mm long; hypanthium (2–)
3–5 mm long, densely to sparsely stipitate-glandular pubescent; bracts glandular, linear, 0.5–1 mm long, densely to sparsely pubescent, the ones subtending
the panicle branches, larger, less glandular, more leaf-like, often with a distinct
stipe; calyx shallowly cupular, the lobes slender, ca. 2.5 mm long, ca. 1 mm wide,
obtuse, densely to sparsely glandular-pubescent with a glandular calycine
squamella protruding from each sepal at or near the point of fusion with the
petals; petals suborbicular, 3–6 mm long, 1–4 mm wide, pale yellow, creamcolored or pink, each with a median adaxial uncinate appendage; stamens ca.
1 mm long, the anthers ca. 0.5 mm long, slightly longer than wide. Pistillate
flowers (fide Cogniaux 1878, 1881, 1916) 1–3; pedicel ca. 6 mm long, densely to
sparsely pubescent; hypanthium ca. 2 mm long, densely to sparsely pubescent;
calyx campanulate, the lobes with a glandular calycine squamella at the point
of fusion between the sepals and the petals; petals strap-shaped, broadened at
the base, cream-colored; styles 3; ovary 5–7 mm long. Fruit (fide Cogniaux
1878, 1881, 1916) subglobose, reddish brown, 7–9 cm wide, pubescent or lightly
glandular-pubescent, the locules 4-seeded; seeds orbicular, compressed, ca. 4
cm long and wide, ca. 1 cm thick, the lateral surface of the woody layer striateverrucose, the outer edge tuberculate.
Distribution and ecology.—Brazil from Ceará southwest to Minas Gerais and
São Paulo.
Selected specimens examined. BRAZIL. Bahia: Ilheus, 1836, Blanchet 2380 (G, F, K, MO, NY, US); km
22 on Ilheus/Itabuna road (BR 415), near Palmoreto, 50 m, 1 Sep 1997, Jardim et al. 1101 (NY). Ceará:
Serra do Araripe, Sep 1828, Gardner 1629 (BM, K). Espírito Santo: Reserva Florestal de Sooretama, 9
ROBINSON AND WUNDERLIN, REVISION OF FEVILLEA
1993
Aug 1965, Belém 1499 (CEPEC, NY); Reserva Florestal da C.V.R.D., Linhares, Estrada Farinha Seca,
Ant. 221, km 1100, 17 Jul 1986, Folli 130 (NY); Reserva Florestal da C.V.R.D., Linhares, Estrada Farinha
Seca, ant. 221, km 1100, 7 Aug 1990, Folli 373 (NY); Reserva Florestal da C.V.R.D., Linhares, 28 Oct
1992, Folli 1715 (NY). Goiás: Formosa, 1814–1817, Bowie & Cunningham 913 (BM). Minas Gerais: near
Viçosa, 8 km from Fazenda de A. Cocerro toward São Miguel, 900 m, 26 Jun 1930, Mexia 4798 (BM, F,
G, MO, NY, US). Paraíba: Cidade Universitária, 6 km SE of Centro de João Pessoa, 7°57'S, 34°53'W, 30–
45 m, 10 Aug 1990, Agra 1165 (MO). Paraná: Barra do Turvo, 10 Oct 1973, Hatschbach 32631 (K, MO,
NY); Barra do Lageado Grande, 31 Aug 1978, Hatschbach 41560 (NY); along road to landing of Porto
Byington on bank of Rio Paraná, 200 m, 26 Jun 1966, Lindeman & de Haas 1778 (NY); Parque Estadual
Vila Rica do Espírito Santo, 18 Feb 1998, Silva s.n. (NY). Pernambuco: Tapera, border of Rio Tapacura,
Oct 1933, Pickel 524 (US). Rio de Janeiro: Gávea, s.d., Glaziou 1344 (BR, US); Serra dos Orgãos, Alto
Macabé, s.d., Glaziou 17010 (NY). São Paulo: Campinas, 27 Aug 1938, Krug 1593 (US).
Fevillea trilobata is most similar to F. cordifolia from which it can be distinguished by its usually angular (vs. rounded) leaf lobes and staminate flowers
with stipitate-glandular trichomes on the hypanthium which are sharply differentiated from the uncinate ones on the pedicel.
Fevillea subgenus Anisosperma (Silva Manso) G. Robinson & Wunderlin, comb.
et stat. nov. BASIONYM: Anisosperma Silva Manso, Enum. Subst. Braz. 38. 1836. TYPE:
Anisosperma passiflora (Vell.) Silva Manso [=Fevillea passiflora Vell.].
Staminate inflorescences of congested panicles or subumbelliform; glandular
calycine squamellae absent; corolla lobes oblong-hastate with a thick glandular
adaxial ridge. Fruit ovate or oblong, subtrigonous, not zonate, the apex apiculate.
Fevillea passiflora Vell., Fl. Flumin., Icon. 10:t. 104. 1831 (“1827”). (Fig. 6).
Anisosperma passiflora (Vell.) Silva Manso, Enum. Subst. Braz. 38. 1836. TYPE: BRAZIL. RIO DE
JANEIRO: (LECTOTYPE: here designated, Vellozo, Fl. Flumin., Icon. 10:t. 104. 1831 (“1827”)).
Vine or liana; stem glabrous or sparsely glandular-pubescent; tendrils glabrous.
Leaves with the blade unlobed, ovate to broadly lanceolate, 5–13 cm long, 4.5–
7.5 cm wide, membranaceous, with a distinct marginal nerve, the apex acute to
acuminate, the base rounded, with 2 small irregular, auriculate glands near the
petiole, the upper and lower surfaces minutely pustulate, sometimes sparsely
glandular-pubescent, the petiole 1–3 cm long. Staminate flowers in a congested
panicle or subumbelliform inflorescence; pedicel (2–)4–5 mm long, sparsely
glandular-pubescent; hypanthium 4–5(–13) mm long, sparsely glandular-pubescent; calyx shallowly cupular, glandular-pubescent, the lobes ca. 2.5 mm
long, lanceolate, acute; petals oblong-hastate, 5–7 mm long, green or cream-colored, the median adaxial ridge glandular, slightly raised, broadest at the base,
gradually tapering to about the center; stamens 1.5–2 mm long, the anthers ca. 1
mm long, slightly longer than wide. Pistillate flowers 2–4 on a short, thick peduncle; styles with the lower part somewhat thickened, the upper part dilated
and broadly obcordate, curved inward longitudinally; ovary 6–9 mm long and
4–5 mm wide, glabrous. Fruit ovoid to oblong, 8–15 cm long, 5–11 cm wide,
subtrigonous, smooth or irregularly verrucose, fleshy with thickened outer
1994
BRIT.ORG/SIDA 21(4)
FIG. 6. Fevillea passiflora. A. Habit, staminate inflorescence (Hatschbach 19205). B. Staminate flower (Hatschbach 9106).
ROBINSON AND WUNDERLIN, REVISION OF FEVILLEA
1995
cortex, the apex short-apiculate; seeds suborbicular, compressed, 3.5–3.5 cm long,
3–4 cm wide, ca. 1.5 cm thick, pale brown, with a thin erose-margined cover.
Distribution and ecology.—Coastal Brazil in southeastern Bahia, Rio de Janeiro, eastern São Paulo, and eastern Paraná. In gallery forests near sea level.
Additional specimens examined. BRAZIL. Bahia: ca. 5 km W of Itamaraju, 20 Sep 1878, Mori et al.
10742 (CEPEC). Paraná: Guaratuba, Rio Cubatão, 27 Dec 1911, Dusén 13640 (F, NY); highway between
Rio Branco do Sul and Cerro Azul along Rio P. Grossa, 26 Apr 1962, Hatschbach 9106 (US); Ribeirinha,
7 May 1968, Hatschbach 19205 (K); Morro do Inglês, 18 Feb 1976, Hatschbach 38090 (K). São Paulo:
Campinas, 1873, Corrêa de Mello s.n. (BR); Cabital, 26 Dec 1941, Pickel 5566 (US); 1816–1821, SaintHilaire D600 (F). Rio de Janeiro: 1894, Glaziou 20335 (BR); Nov 1987, Glaziou 10870 (K); Cantagalo,
1859, Peckolt 8 (BR); Cantagalo, 1861, Peckolt s.n. (BR); Teresópolis, Serra dos Orgãos, 27 Feb 1887,
Schenck 2898 (BR). Without precise locality: 1859, Peckolt s.n. (BR); s.d., Martius s.n. (BR).
EXCLUDED NAMES
Fevillea deltoidea Cogn., in Martius, Fl. Bras. 6(4):119. 1878. [=Pteropepon deltoideus
(Cogn.) Cogn.].
Fevillea monosperma Vell., Fl. Flumin., Icon. 10:t. 103. 1831 (“1827”). [=Pteropepon
monospermus (Vell.) Cogn.].
Fevillea pedata Smith ex Sims, Bot. Mag. t. 2681. 1826.
[=Telfairia pedata (Smith ex
Sims) Hooker].
Fevillea punctata (L.) Poir., in Lamarck, Encycl. 4:418. 1796.
BASIONYM: Bryonia
punctata L., Demonstr. Pl. 26. 1753. TYPE: Herb. Linn. No. 1180.1 (two sheets); apparently a mixed
collection, possibly a Trichosanthes and a Momordica.
Fevillea tamnifolia Kunth, in Humboldt, Bonpland & Kunth, Nov. Gen. Sp. 7:175.
1825. [=Sicydium tamnifolium (Kunth) Cogn.].
Fevillea trilobata Reichard, Syst. Pl. 4:253. 1780, nom. illegit.; non L., 1753.
(BASIONYM: Bryonia punctata L., 1753.) [See Fevillea punctata above.]
ACKNOWLEDGMENTS
We gratefully acknowledge the curators of BM, BR, CEPEC, F, G, K, M, MO, NY,
US, and USF for making specimens available to us for study. We thank Bruce
Hansen (USF) for his many helpful suggestions on the manuscript and Kathleen Hotchkiss (USF) for assistance with graphics. We also thank Michael Nee
(NY) and an anonymous reviewer for their helpful comments.
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